FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term hereditary spastic paraplegia 90B ID (Ontology) DOID:0070460 (Human Disease)
Definition A hereditary spastic paraplegia characterized by motor impairment and progressive lower limb spasticity that has_material_basis_in homozygous mutation in the SPTSSA gene on chromosome 14q13.1.
Also Known As "autosomal recessive spastic paraplegia 90B" ; "SPG90B"
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 Genes
 hereditary spastic paraplegia 90B       1
 for disease ribbon | hereditary spastic paraplegia 90B       1
 model of | hereditary spastic paraplegia 90B       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease_____
paraplegia                         |
 |__hereditary spastic paraplegia__|
                                   hereditary spastic paraplegia 90B  1 rec.
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Is a autosomal dominant disease
hereditary spastic paraplegia
Part of
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Synonyms
  • "autosomal recessive spastic paraplegia 90B" EXACT
    "SPG90B" EXACT OMO:0003012
Secondary IDs
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MIM:620417